Connexin: Difference between revisions
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*'''Connexin 26''' participates in K+ transport in sensory hair cells in the ear and its mutations are causes of deafness<ref>pmid 9285800</ref> | *'''Connexin 26''' participates in K+ transport in sensory hair cells in the ear and its mutations are causes of deafness<ref>pmid 9285800</ref> | ||
*'''Connexin 31''' mutations are associated with skin and auditory system disorders<ref>PMID 16549784</ref> | *'''Connexin 31''' mutations are associated with skin and auditory system disorders<ref>PMID 16549784</ref> | ||
*'''Connexin 32''' is found in the peripheral nervous system and its mutations are associated with Charcot-Marie-Tooth disease<ref>PMID 30042657</ref> | |||